Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene 783766005
SNOMED CT code
SNOMED code | 783766005 |
---|---|
name | Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene |
status | active |
date introduced | 2019-07-31 |
fully specified name(s) | Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder) |
synonyms |
|
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Erythrocyte 41898006 |
attributes - group2 | |
Interprets | Red blood cell count 14089001 |
Has interpretation | Above reference range 281302008 |
attributes - group3 | |
Interprets | Hematology procedure 33468001 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Red blood cell disorder 38292009 Hereditary red blood cell disorder 414394009 Familial erythrocytosis 17342003 Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene 783766005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene 783766005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene 783766005 |
ancestors | sorted most to least specific
|
cpt crosswalks |
Thank you for choosing Find-A-Code, please Sign In to remove ads.